scStateDynamics: deciphering the drug-responsive tumor cell state dynamics by modeling single-cell level expression changes

Understanding tumor cell heterogeneity and plasticity is crucial for overcoming drug resistance. Single-cell technologies enable analyzing cell states at a given condition, but catenating static cell snapshots to characterize dynamic drug responses remains challenging. Here, we propose scStateDynamics, an algorithm to infer tumor cell state dynamics and identify common drug effects by modeling single-cell level gene expression changes. Its reliability is validated on both simulated and lineage tracing data. Application to real tumor drug treatment datasets identifies more subtle cell subclusters with different drug responses beyond static transcriptome similarity and disentangles drug action mechanisms from the cell-level expression changes.

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Publication Details

Journal
Genome biology
Published
2024-11-21
DOI
https://doi.org/10.1186/s13059-024-03436-y
Citations
2
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
0.47
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article

scStateDynamics: deciphering the drug-responsive tumor cell state dynamics by modeling single-cell level expression changes

Jin Gu, Qifan Hu, Nan Yan, Xinqi Li et al.
2 citations
Genome biology
Single-cell and spatial transcriptomics
0.47
article

scStateDynamics: deciphering the drug-responsive tumor cell state dynamics by modeling single-cell level expression changes

Jin Gu, Qifan Hu, Nan Yan, Xinqi Li, Xuegong Zhang, Fan Yang, Dongfang Wang, Wenbo Guo, Jianhua Yao
article en
2 citations

Abstract

Understanding tumor cell heterogeneity and plasticity is crucial for overcoming drug resistance. Single-cell technologies enable analyzing cell states at a given condition, but catenating static cell snapshots to characterize dynamic drug responses remains challenging. Here, we propose scStateDynamics, an algorithm to infer tumor cell state dynamics and identify common drug effects by modeling single-cell level gene expression changes. Its reliability is validated on both simulated and lineage tracing data. Application to real tumor drug treatment datasets identifies more subtle cell subclusters with different drug responses beyond static transcriptome similarity and disentangles drug action mechanisms from the cell-level expression changes.

Genome biologyVol. 25(1)
Peking University (CN), Tencent (China) (CN), Tsinghua University (CN)
Good health and well-being
Openalex Percentile: Top 34%
Single-cell and spatial transcriptomics
0.47
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